Long‐Term Corticosteroid‐Sparing Immunosuppression for Cardiac Sarcoidosis

Author:

Rosenthal David G.1,Parwani Purvi1,Murray Tyler O.1,Petek Bradley J.2,Benn Bryan S.3,De Marco Teresa1,Gerstenfeld Edward P.1,Janmohamed Munir1,Klein Liviu1,Lee Byron K.1,Moss Joshua D.1,Scheinman Melvin M.1,Hsia Henry H.1,Selby Van1,Koth Laura L.3,Pampaloni Miguel H.4,Zikherman Julie5,Vedantham Vasanth1

Affiliation:

1. Division of Cardiology Department of Medicine University of California, San Francisco San Francisco CA

2. Department of Medicine Massachusetts General Hospital Boston MA

3. Division of Pulmonary and Critical Care Department of Medicine University of California, San Francisco San Francisco CA

4. Division of Nuclear Medicine Department of Radiology University of California, San Francisco San Francisco CA

5. Division of Rheumatology Department of Medicine University of California, San Francisco San Francisco CA

Abstract

Background Long‐term corticosteroid therapy is the standard of care for treatment of cardiac sarcoidosis ( CS ). The efficacy of long‐term corticosteroid‐sparing immunosuppression in CS is unknown. The goal of this study was to assess the efficacy of methotrexate with or without adalimumab for long‐term disease suppression in CS , and to assess recurrence and adverse event rates after immunosuppression discontinuation. Methods and Results Retrospective chart review identified treatment‐naive CS patients at a single academic medical center who received corticosteroid‐sparing maintenance therapy. Demographics, cardiac uptake of 18‐fluorodeoxyglucose, and adverse cardiac events were compared before and during treatment and between those with persistent or interrupted immunosuppression. Twenty‐eight CS patients were followed for a mean 4.1 ( SD 1.5) years. Twenty‐five patients received 4 to 8 weeks of high‐dose prednisone (>30 mg/day), followed by taper and maintenance therapy with methotrexate±low‐dose prednisone (low‐dose prednisone, <10 mg/day). Adalimumab was added in 19 patients with persistently active CS or in those with intolerance to methotrexate. Methotrexate±low‐dose prednisone resulted in initial reduction (88%) or elimination (60%) of 18‐fluorodeoxyglucose uptake, and patients receiving adalimumab‐containing regimens experienced improved (84%) or resolved (63%) 18‐fluorodeoxyglucose uptake. Radiologic relapse occurred in 8 of 9 patients after immunosuppression cessation, 4 patients on methotrexate‐containing regimens, and in no patients on adalimumab‐containing regimens. Conclusions Corticosteroid‐sparing regimens containing methotrexate with or without adalimumab is an effective maintenance therapy in patients after an initial response is confirmed. Disease recurrence in patients on and off immunosuppression support need for ongoing radiologic surveillance regardless of immunosuppression regimen.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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